Literature DB >> 9914413

Neural expression of hikaru genki protein during embryonic and larval development of Drosophila melanogaster.

M Hoshino1, E Suzuki, T Miyake, M Sone, A Komatsu, Y Nabeshima, C Hama.   

Abstract

Hikaru genki (HIG) is a putative secreted protein of Drosophila that belongs to immunoglobulin and complement-binding protein superfamilies. Previous studies reported that, during pupal and adult stages, HIG protein is synthesized in subsets of neurons and appears to be secreted to the synaptic clefts of neuron-neuron synapses in the central nervous system (CNS). Here we report the analyses of distribution patterns of HIG protein at embryonic and larval stages. In embryos, HIG was mainly observed in subsets of neurons of the CNS that include pCC interneurons and RP5 motorneurons. At third instar larval stage, this protein was detected in a limited number of cells in the brain and ventral nerve cord. Among them are the motorneurons that extend their axons to make neuromuscular junctions on body wall muscle 8. Immunoelectron microscopy showed that these axonal processes as well as the neuromuscular terminals contain numerous vesicles with HIG staining, suggesting that HIG is in a pathway of secretion at this stage. Some neurosecretory cells were also found to express this protein. These data suggest that HIG functions in the nervous system through most developmental stages and may serve as a secreted signalling molecule to modulate the property of synapses or the physiology of the postsynaptic cells.

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Year:  1999        PMID: 9914413     DOI: 10.1007/s004270050221

Source DB:  PubMed          Journal:  Dev Genes Evol        ISSN: 0949-944X            Impact factor:   0.900


  7 in total

Review 1.  Extracellular matrix and its receptors in Drosophila neural development.

Authors:  Kendal Broadie; Stefan Baumgartner; Andreas Prokop
Journal:  Dev Neurobiol       Date:  2011-11       Impact factor: 3.964

2.  Genomic sequence of a 320-kb segment of the Z chromosome of Bombyx mori containing a kettin ortholog.

Authors:  Y Koike; K Mita; M G Suzuki; S Maeda; H Abe; K Osoegawa; P J deJong; T Shimada
Journal:  Mol Genet Genomics       Date:  2003-03-12       Impact factor: 3.291

3.  Regulatory role of rpL3 in cell response to nucleolar stress induced by Act D in tumor cells lacking functional p53.

Authors:  Annapina Russo; Valentina Pagliara; Francesco Albano; Davide Esposito; Vinay Sagar; Fabrizio Loreni; Carlo Irace; Rita Santamaria; Giulia Russo
Journal:  Cell Cycle       Date:  2016       Impact factor: 4.534

4.  Presynaptic establishment of the synaptic cleft extracellular matrix is required for post-synaptic differentiation.

Authors:  Jeffrey Rohrbough; Emma Rushton; Elvin Woodruff; Tim Fergestad; Krishanthan Vigneswaran; Kendal Broadie
Journal:  Genes Dev       Date:  2007-09-27       Impact factor: 11.361

5.  A secreted complement-control-related protein ensures acetylcholine receptor clustering.

Authors:  Marie Gendrel; Georgia Rapti; Janet E Richmond; Jean-Louis Bessereau
Journal:  Nature       Date:  2009-09-30       Impact factor: 49.962

6.  The Matrix Proteins Hasp and Hig Exhibit Segregated Distribution within Synaptic Clefts and Play Distinct Roles in Synaptogenesis.

Authors:  Minoru Nakayama; Emiko Suzuki; Shin-ichi Tsunoda; Chihiro Hama
Journal:  J Neurosci       Date:  2016-01-13       Impact factor: 6.167

7.  Loss of yata, a novel gene regulating the subcellular localization of APPL, induces deterioration of neural tissues and lifespan shortening.

Authors:  Masaki Sone; Atsuko Uchida; Ayumi Komatsu; Emiko Suzuki; Ikue Ibuki; Megumi Asada; Hiroki Shiwaku; Takuya Tamura; Mikio Hoshino; Hitoshi Okazawa; Yo-ichi Nabeshima
Journal:  PLoS One       Date:  2009-02-11       Impact factor: 3.240

  7 in total

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